Medical Device Manufacturer · FR , Marseille

Idmed

3 submissions · 3 cleared · Since 2018
3
Total
3
Cleared
0
Denied

Idmed — FDA 510(k) Submissions

Idmed has submitted 3 FDA 510(k) premarket notifications since 2018, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Nerve, Peripheral, Electric, Cuff, Tracheal Tube, Inflatable . Use the specialty filter in the sidebar to narrow results.

3 devices
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All3 Anesthesiology 3